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用于检测副黏液病毒的全家族 RT-PCR 检测法及其在大规模监测研究中的应用。

A family-wide RT-PCR assay for detection of paramyxoviruses and application to a large-scale surveillance study.

机构信息

Department of Virology, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

PLoS One. 2012;7(4):e34961. doi: 10.1371/journal.pone.0034961. Epub 2012 Apr 4.

Abstract

Family-wide molecular diagnostic assays are valuable tools for initial identification of viruses during outbreaks and to limit costs of surveillance studies. Recent discoveries of paramyxoviruses have called for such assay that is able to detect all known and unknown paramyxoviruses in one round of PCR amplification. We have developed a RT-PCR assay consisting of a single degenerate primer set, able to detect all members of the Paramyxoviridae family including all virus genera within the subfamilies Paramyxovirinae and Pneumovirinae. Primers anneal to domain III of the polymerase gene, with the 3' end of the reverse primer annealing to the conserved motif GDNQ, which is proposed to be the active site for nucleotide polymerization. The assay was fully optimized and was shown to indeed detect all available paramyxoviruses tested. Clinical specimens from hospitalized patients that tested positive for known paramyxoviruses in conventional assays were also detected with the novel family-wide test. A high-throughput fluorescence-based RT-PCR version of the assay was developed for screening large numbers of specimens. A large number of samples collected from wild birds was tested, resulting in the detection of avian paramyxoviruses type 1 in both barnacle and white-fronted geese, and type 8 in barnacle geese. Avian metapneumovirus type C was found for the first time in Europe in mallards, greylag geese and common gulls. The single round family-wide RT-PCR assay described here is a useful tool for the detection of known and unknown paramyxoviruses, and screening of large sample collections from humans and animals.

摘要

全家族分子诊断检测对于暴发期间初始鉴定病毒以及限制监测研究成本非常有用。最近发现的副粘病毒要求进行此类检测,以在一轮 PCR 扩增中检测所有已知和未知的副粘病毒。我们开发了一种 RT-PCR 检测方法,由单个简并引物组组成,能够检测副粘病毒科的所有成员,包括副粘病毒亚科和肺病毒亚科内的所有病毒属。引物与聚合酶基因的结构域 III 退火,反向引物的 3' 端与保守基序 GDNQ 退火,该基序被提议为核苷酸聚合的活性位点。该检测方法已进行了全面优化,确实可以检测到所有已测试的可用副粘病毒。在常规检测中对已知副粘病毒呈阳性的住院患者的临床标本也可通过新型全家族检测方法检测到。针对大量标本开发了基于高通量荧光的 RT-PCR 版本检测。对大量采集自野生鸟类的样本进行了测试,结果在大滨鹬、白头鹮鹳和普通海鸥中检测到了 1 型禽副粘病毒,在大滨鹬中检测到了 8 型禽副粘病毒。在欧洲首次在绿头鸭、灰雁和普通海鸥中发现了 C 型禽偏肺病毒。本文描述的单轮全家族 RT-PCR 检测方法是一种用于检测已知和未知副粘病毒以及筛选人类和动物大量样本的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e77/3319594/a44f98519425/pone.0034961.g001.jpg

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